Senior Clinical Programmer

IQVIA•Durham, NC

1d•$88,300 - $220,900

About The Position

This Clinical Programmer role at IQVIA supports Risk‑Based Quality Management by developing and validating KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring platform. The position blends programming and analytics to transform complex clinical and operational data into actionable insights, partnering closely with Clinical Monitoring, Data Management, Biostatistics, and RBQM leads. Strong clinical data expertise and proficiency in SAS and other analytical tools are essential for success. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Requirements

Strong clinical data expertise
Proficiency in SAS (mandatory)
Strong understanding of clinical trial data structures, including SDTM, EDC‑derived datasets, operational metrics, and vendor‑sourced data
Proficiency in data analysis and programming tools, including SQL, Python, R, Spotfire, or equivalent analytical platforms
Ability to interpret complex analytical and statistical outputs and convert them into actionable insights

Nice To Haves

Hands‑on experience with CluePoints CM, KRI/QTL development, and Risk‑Based Quality Management (RBQM) frameworks

Responsibilities

Develop and document requirements for the design of Key Risk Indicators (KRIs) and Quality Tolerance Limits (QTLs) based on Critical‑to‑Quality (CtQ) factors and key study documents (e.g., protocol, CRF Completion Guidelines, data flow specifications).
Program, configure, and validate KRIs, QTLs, and other risk signals within the CluePoints Central Monitoring (CM) platform, ensuring accurate and reliable representation of study risks.
Collaborate closely with Clinical Monitoring, Data Management, RBQM Leads, Biostatistics, and Study Teams to translate analytical insights into actionable risk mitigation strategies and study interventions.
Prepare dashboards, analytics summaries, risk reports, and data visualizations to clearly communicate findings to study teams and cross‑functional stakeholders.